Service
Study design and sample size
This is the only point at which everything is still fixable. I help you size your study, choose the right variables and write the analysis plan — before collection locks in your options.
Who it is for
This service comes in up front, when the data does not exist yet. It is also the least requested, even though it is the one that prevents the most damage: an under-sized study cannot be rescued afterwards.
- Clinical researchers submitting a protocol
- PhD students at the start of their thesis
- Teams preparing an ethics committee application
- Applicants who must justify a funding request
- Companies about to run a survey or an A/B test
- Labs planning a measurement campaign
The problem it solves
Most analyses that fail do not fail at the analysis stage. They fail at collection: too few subjects to detect the effect sought, a confounding variable nobody thought to measure, two groups formed in a way that makes them no longer comparable.
These mistakes have an unpleasant property: they are irreversible. No statistical method, however sophisticated, recovers information that was never collected. You can only note the damage and publish an inconclusive result.
A few hours of design up front cost a fraction of a collection redone — when redoing it is even possible.
- An ethics committee wants the sample size justified
- You do not know how many subjects to include
- You are unsure which variables to measure
- You have to write the "statistical analysis" section of a protocol
- A funder asks for the expected statistical power
- You want to avoid repeating the last study's mistake
What you get
Deliverables are written to drop straight into your protocol, your ethics application or your funding request.
- The sample size calculation, with its assumptions spelled out
- The power analysis and alternative scenarios
- A written, dated and versioned statistical analysis plan
- The list of variables to measure, and why each one
- Recommendations on group allocation and randomisation
- A "statistical methods" section ready for your protocol
How it works
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Research question
We start from what you want to demonstrate and turn it into a testable hypothesis. That step determines everything else.
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Feasibility
How many subjects can you realistically recruit, in what time, on what budget? The constraints are part of the calculation.
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Sizing
Sample size computed under several effect scenarios, so you choose with full knowledge of the trade-off.
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Analysis plan
The plan and the methods section written up, ready to attach to your application.
Concrete examples
Methodological illustrations of the questions handled at this stage.
How many patients to include?
Detecting a clinically meaningful difference with 80% power: the calculation, its assumptions, and what happens if recruitment falls short.
Which variables to measure?
Identifying the confounders to collect up front. A variable missed at this stage can never be added to the model later.
How to form the groups?
Simple, stratified or block randomisation — and what each choice implies for the analysis that follows.
A usable questionnaire
Wording the questions and response scales so that the resulting data can actually be analysed.
Sizing an A/B test
How many visitors and how long before you can conclude, rather than stopping the test as soon as the curve looks good.
Interim analyses
Planning to look at results mid-study without invalidating the final test: the rules are set beforehand, not after.
Frequently asked questions
Is this really necessary for a small study?
I have no idea what effect to expect. How can a sample size be calculated?
Collection has already started. Is it too late?
Will the ethics committee accept the calculation?
How long does it take?
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Describe your need in a few lines, or book a first no-commitment call. I will tell you straight if I am the right person for it.